Package 72189-482-30

Brand: quetiapine fumarate er

Generic: quetiapine fumarate er
NDC Package

Package Facts

Identity

Package NDC 72189-482-30
Digits Only 7218948230
Product NDC 72189-482
Product ID 72189-482_2c4e1a9a-24e9-0784-e063-6394a90ac55b
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-482-30)

Marketing

Marketing Status
Marketed Since 2023-06-01
Brand quetiapine fumarate er
Generic quetiapine fumarate er
Sample Package No

Linked Drug Pages (1)

Quetiapine Fumarate ER ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4e1a9a-24e9-0784-e063-6394a90ac55b", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721791"], "spl_set_id": ["fd12e3cb-8b9b-4ea0-e053-6294a90a4e7a"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-482-30)", "package_ndc": "72189-482-30", "marketing_start_date": "20230601"}], "brand_name": "Quetiapine Fumarate ER", "product_id": "72189-482_2c4e1a9a-24e9-0784-e063-6394a90ac55b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-482", "generic_name": "Quetiapine Fumarate ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate ER", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA090681", "marketing_category": "ANDA", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}